Author

Yaron Galanty

University of CambridgeORCID 0000-0001-7167-9004Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cell Biology· 1 Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Assay:DNA methylation· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:whole-genome sequencing· 2 Approach:deep learning· 1 Research Focus:gene regulatory network inference· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Petra BeliiD· 2 shared Shane A McKeeiD· 2 shared Stephen P. JacksoniD· 2 shared Aldo S. BaderiD· 1 shared Alexander J. Strong· 1 shared Amanda K. ChapliniD· 1 shared Andrew R. Bassett· 1 shared Anirban MajumdariD· 1 shared

Activity by Year

2018-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 22 mutual co-author links

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2 shared papersGenetics

Petra BeliORCID

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3 papers

Recent·Most cited

GeneticsEMBO Molecular MedicinePeer-reviewedDec 19, 2025

Loss of CTLH component MAEA impairs DNA repair and replication and leads to developmental delay

Soren H. Hough, Satpal S. Jhujh, Samah W. Awwad…·Stephen P. Jackson

The paper identifies MAEA as a critical regulator of DNA repair and replication, with loss of function causing developmental delay and neurodevelopmental deficits.

2 citations

humanDNA methylation

𝕏 PostBluesky

Molecular BiologybioRxivPreprintJun 16, 2025

UFMylation orchestrates chromatin engagement of core NHEJ components to promote DNA double-strand break repair

Zijuan Wang, Benjamin M. Foster, Isabelle Cristine da Costa…·Christine K. Schmidt

The paper identifies UFM1 as a regulator of NHEJ by orchestrating chromatin engagement of core components, linking UFMylation defects to DSB repair defects.

DOI 10.1101/2025.06.16.659844

humanexperimental assay

𝕏 PostBluesky

Cell BiologybioRxivPreprintAug 25, 2018

Mutations generated by repair of Cas9-induced double strand breaks are predictable from surrounding sequence

Felicity Allen, Luca Crepaldi, Clara Alsinet…·Leopold Parts

The paper predicts Cas9-induced mutation outcomes based on surrounding DNA sequence using data from over 1 billion mutational outcomes.

DOI 10.1101/400341

DNA methylationwhole-genome sequencing

𝕏 PostBluesky